Phase 2 OCD Trial, Recruiting (NCT04899687)

Phase 2 OCD Trial, Recruiting NCT04899687 Sponsor: Stanford University Condition: OCD

Printed from Voxsanity (voxsanity.com.au) — NCT04899687 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.

Back to Ocd

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

You have been diagnosed with obsessive-compulsive disorder (OCD), body dysmorphic disorder (BDD), illness anxiety disorder (IAD), or somatic symptom disorder (SSD)
You currently live in California
You are able to understand and agree to participate in the study on your own

Who may not be able to join:

You have been diagnosed with bipolar disorder or a psychotic disorder
You currently have a moderate or severe problem with alcohol or drug use, or have had a severe substance use problem at any point in your life
You are currently pregnant or breastfeeding
You are taking any prescribed mental health medications, except for fluoxetine, within the 2 weeks before the study begins
You have recently started a specific type of therapy for OCD called exposure and response prevention (ExRP) within the past 2 months before the study begins

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.

Last synced 28 July 2026

Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Peter J van Roessel, MD PhD, Stanford University

Phone: 650 497 2578

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Voxsanity

Clinical trials and treatments, explained plainly · voxsanity.com.au

Date:

To: My Doctor

Re: Clinical trial enquiry

I am writing to enquire about the following clinical trial which may be relevant to my care:

Trial: NCT04899687

Sponsor: Stanford University

Phase: Phase 2

Status: Recruiting

Condition: OCD

Trial contact: 650 497 2578

More information: https://clinicaltrials.gov/study/NCT04899687

Eligibility summary (AI generated)

Written by an AI model from the ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

You have been diagnosed with obsessive-compulsive disorder (OCD), body dysmorphic disorder (BDD), illness anxiety disorder (IAD), or somatic symptom disorder (SSD)
You currently live in California
You are able to understand and agree to participate in the study on your own

Who may not be able to join:

You have been diagnosed with bipolar disorder or a psychotic disorder
You currently have a moderate or severe problem with alcohol or drug use, or have had a severe substance use problem at any point in your life
You are currently pregnant or breastfeeding
You are taking any prescribed mental health medications, except for fluoxetine, within the 2 weeks before the study begins
You have recently started a specific type of therapy for OCD called exposure and response prevention (ExRP) within the past 2 months before the study begins

Important: Always verify eligibility with the trial site directly before applying.

Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.

This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 28 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.

Trial details

Status

Recruiting

Phase

Phase 2

Sponsor

Stanford University

Registry

ClinicalTrials.gov

Start date

20 January 2022

Est. completion

1 April 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Improvement in OCD or related disorder symptoms as measured by the Y-BOCS

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov